MT 10 - TC 66/MT 10

IEC 61010-2-081:2019 applies to automatic and semi-automatic laboratory equipment for analysis and other purposes. Automatic and semi-automatic laboratory equipment consists of instruments or systems for measuring or modifying one or more characteristics or parameters of samples, performing the complete process or parts of the process without manual intervention. Equipment forming part of such a system is within the scope of this document. This third edition cancels and replaces the second edition published in 2015. This edition constitutes a technical revision. This edition includes the following significant technical changes with respect to the previous edition:
- adaptation of changes introduced by Amendment 1 of IEC 61010-1:2010;
- added tolerance for stability of AC voltage test equipment to Clause 6.
It has the status of a group safety publication in accordance with IEC Guide 104.

IEC 61010-2-051:2018 is applicable to electrically operated laboratory equipment and its accessories for mechanical mixing and stirring, where mechanical energy influences the shape or size or homogeneity of materials and their accessories. Such devices can contain heating elements. It has the status of a group safety publication in accordance with IEC Guide 104. This fourth edition cancels and replaces the third edition published in 2015. This edition constitutes a technical revision. This edition includes the following significant technical changes with respect to the previous edition:
- adaptation of changes introduced by Amendment 1 of IEC 61010-1;
- added tolerance for stability of AC voltage test equipment to Clause 6;
- added required assessment for equipment intended to be used with flammable, hazardous, or toxic fluids to Clause 17.
This Part 2-051 is intended to be used in conjunction with IEC 61010-1. It was established on the basis of the third edition (2010) and its Amendment 1 (2016).

IEC 61010-2-101:2018 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. It has the status of a group safety publication, as specified in IEC Guide 104. This document has been prepared in close collaboration with Working Group CENELEC BTTF 88.1. This third edition cancels and replaces the second edition published in 2015. This edition constitutes a technical revision. This edition includes the following significant technical changes with respect to the previous edition:
- adaptation of changes introduced by Amendment 1 of IEC 61010-1;
- added tolerance for stability of AC voltage test equipment to Clause 6.
This Part 2-101 is intended to be used in conjunction with IEC 61010-1. It was established on the basis of the third edition (2010) and its Amendment 1 (2016).

IEC 61010-2-061:2018 applies to electrically powered laboratory atomic spectro­meters with thermal atomization. It has the status of a group safety publication in accordance with IEC Guide 104. This fourth edition cancels and replaces the third edition published in 2015. This edition constitutes a technical revision. This edition includes the following significant technical changes with respect to the previous edition:
- adaptation of changes introduced by Amendment 1 of IEC 61010-1;
- added tolerance for stability of AC voltage test equipment to Clause 6;
- added requirement for interlock systems containing electric/electronic or programmable components to Clause 15.

IEC 61010-2-061:2015 applies to electrically powered laboratory atomic spectrometers with thermal atomization. It has the status of a group safety publication in accordance with IEC Guide 104. This third edition cancels and replaces the second edition published in 2003. It constitutes a technical revision and includes the following change from the second edition:
- exclusion of equipment, whose size and weight make unintentional movement unlikely, from the drop test in Clause 8.
- notes have been re-phrased according to ISO/IEC Directives.
This publication is to be read in conjunction with IEC 61010-1:2010.

IEC 61010-2-051:2015 is applicable to electrically operated laboratory equipment and its accessories for mechanical mixing and stirring, where mechanical energy influences the shape or size or homogeneity of materials and their accessories. Such devices may contain heating elements. It has the status of a group safety publication in accordance with IEC Guide 104. This third edition cancels and replaces the second edition published in 2003. It constitutes a technical revision and includes the following change from the second edition:
- exclusion of equipment, whose size and weight make unintentional movement unlikely, from the drop test in Clause 8,
- added requirement for interlock systems containing electric/electronic or programmable components to Clause 15,
- notes have been re-phrased according to ISO/IEC Directives.
This publication is to be read in conjunction with IEC 61010-1:2010.

IEC 61010-2-081:2015 applies to automatic and semi-automatic laboratory equipment for analysis and other purposes. Automatic and semi-automatic laboratory equipment consists of instruments or systems for measuring or modifying one or more characteristics or parameters of samples, performing the complete process or parts of the process without manual intervention. Equipment forming part of such a system is within the scope of this standard. This second edition cancels and replaces the first edition published in 2003. It constitutes a technical revision and includes the following significant changes from the first edition, as well as numerous other changes:
- excluded IEC 61010-2-101 (IVD Equipment) from scope. This separates IEC 61010-2-081 and IEC 61010-2-101 equipment;
- added biological risks symbol to Table 1 in Clause 5;
- added requirement for statement on hazardous substances and gases in Instructions for Use to Clause 5;
- Added marking requirement for flow direction to Clause 5;
- added requirement for OPERATOR maintenance instructions to Clause 7;
- excluded equipment whose size and weight make unintentional movement unlikely from drop test in Clause 8;
- added requirement for biohazard marking to Clause 13;
- added requirement for interlock systems containing electric/electronic or programmable components to Clause 15.
It has the status of a group safety publication in accordance with IEC Guide 104.
This publication is to be read in conjunction with IEC 61010-1:2010.

IEC 61010-2-101:2015 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. It has the status of a group safety function, as specified in IEC Guide 104. This standard has been prepared in close collaboration with Working Group CENELEC BTTF 88.1. This second edition cancels and replaces the first edition published in 2002. It constitutes a technical revision and includes the following significant changes from the first edition, as well as numerous other changes:
- excluded IEC 61010-2-081 (general laboratory equipment) from the scope. This separates IEC 61010-2-081 and IEC 61010-2-101 equipment;
- updated Biohazard and Lot symbols in Table 1 in Clause 5;
- added requirement for within expiration consumables and authorized representative details in Instructions for Use to Clause 5;
- added requirement for gas or liquid markings and ratings to Clause 5;
- added requirement to include OPERATOR instructions to deal with consumable or sample spills, jams or breakage inside equipment, disposal of hazardous waste, personal protection, RISK reduction procedures relating to flammable liquids, burns from surfaces, and loading and unloading of sample and reagents in Instructions for Use to Clause 5;
- added requirement for manufacturer to provide instructions on equipment transport, storage and removal from use to Clause 5;
- added normative reference ISO 18113-5 for instructions for use of self-test IVD medical equipment in Clause 5;
- added requirement for OPERATOR maintenance instructions to Clause 7;
- added requirements for sample zones and loading zones to Clause 7;
- excluded equipment whose size and weight make unintentional movement unlikely from drop test in Clause 8;
- added requirement for biohazard marking to Clause 13;
- added requirement for interlock systems containing electric/electronic or programmable components to Clause 15;
- added informative reference to Usability standard IEC 62366 to Clause 16;
- replaced Clause 17 with requirements of ISO 14971 for RISK assessment.
- Annex BB Instructions for use for self-testing IVD Medical Equipment deleted and a reference given to ISO 18113-5 in Clause 5.
This publication is to be read in conjunction with IEC 61010-1:2010.

IEC 61010-2-010:2014 specifies safety requirements for electrically powered laboratory equipment for the heating of materials, where the heating of materials is one of the functions of the equipment. This third edition cancels and replaces the second edition published in 2003. It constitutes a technical revision and includes the following significant changes from the second edition, as well as numerous other changes:
- added a definition for HEAT TRANSFER MEDIUM to Clause 3;
- added a symbol for FLAMMABLE LIQUID to Table 1 in Clause 5;
- added a requirement for instructions pertaining to ventilation in Clause 5;
- modified the requirements for humidity preconditioning in Clause 6;
- added requirements for equipment containing or using flammable liquids to Clause 9;
- added requirements for over-temperature protection devices to Clause 10.
It has the status of a horizontal standard in accordance with IEC Guide 104.
This publication is to be read in conjunction with IEC 61010-1:2010.

This part of IEC 61010 applies only to electrically powered laboratory equipment for the heating of materials, where the heating of materials is the only function or is one of several functions of the equipment

Applies to equipment intended for in vitro diagnostic (IVD) medical purposes. This is used for the examination of specimens, including blood and tissue samples, derived from the human body. The standard also covers self-test IVD medical equipment for use by lay persons.